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Frontier Clinical Research, Total:79 items.
In the international standard classification, Frontier Clinical Research involves: Vocabularies, Laboratory medicine, Medical equipment, Birth control. Mechanical contraceptives, Medical sciences and health care facilities in general, Biology. Botany. Zoology, Dentistry, Hospital equipment, Labour. Employment, Pharmaceutics, Applications of information technology.
Group Standards of the People's Republic of China, Frontier Clinical Research
- T/CAV 001-2023 Terms used in vaccine preclinical research
- T/CACM 015.12-2017 Chinese medicine clinical research verification standards
- T/CAAM 0007-2022 Guidelines for Acupuncture and Moxibustion Clinical Research Registration
- T/SDHCST 003-2023 Pre-dose Quality Testing of Test Substances in Non-clinical Studies of the Cell Therapy Medical Products
- T/CACM 015.10-2017 Drug Administration Standards for Clinical Research of Traditional Chinese Medicine
- T/CACM 015.8-2017 Standards for management of clinical research documents of traditional Chinese medicine
- T/ZJPA 002-2024 Clinical Research Coordinator (CRC) Training Requirement
- T/CACM 015.3-2017 Quality Control Standards for Clinical Research of Traditional Chinese Medicine
- T/CGCPU 001-2015 Guidance for clinical research coordinator profession practice
- T/CRHA 067-2024 The guidelines of clinical research telephone-based follow-up
- T/CGDF 00042-2024 Standard for allergic diseases clinical research base construction
- T/CMBA 022-2024 Construction and management specification for developing clinical research unit
- T/CAAM 0002-2022 Acupuncture and moxibustion clinical research adverse event recording specification
SCC, Frontier Clinical Research
- BS EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects-Clinical investigation plans
- AS ISO 14155:2002 Clinical investigation of medical devices
- NS-EN ISO 14155-2:2003 Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans (ISO 14155-2:2003)
- UNE-EN ISO 14155-2:2004 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
- DANSK DS/EN ISO 14155/AC:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
- DANSK DS/EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- DANSK DS/ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice
- AAMI/ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice
- ISO 14155:2020 Plus Redline Clinical investigation of medical devices for human subjects - Good clinical practice
- 08/30116059 DC BS ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
- UNE-EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
- AENOR UNE-EN ISO 14155:2012 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
- NS-EN ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
- DANSK DS/EN ISO 14155:2020 Clinical investigation of medical devices for human subjects – Good clinical practice (ISO 14155:2020)
- NS-EN ISO 14155:2020 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
- NS-EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003)
- BS EN 540:1993 Clinical investigation of medical devices for human subjects
- NS-EN 540:1993 Clinical investigation of medical devices for human subjects
- DIN EN ISO 14155 E:2018 Draft Document - Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2018); German and English version prEN ISO 14155:2018
Korean Agency for Technology and Standards (KATS), Frontier Clinical Research
- KS P ISO 14155-2-2007(2012) Clinical investigation of medical devices for human subjects－Part 2：Clinical investigation plans
- KS P ISO 14155-2-2019 Clinical investigation of medical devices for human subjects－Part 2：Clinical investigation plans
VN-TCVN, Frontier Clinical Research
- TCVN 7740-2-2007 Clinical investigation of medical devices for human subjects.Part 2: Clinical investigation plans
未注明發(fā)布機構, Frontier Clinical Research
European Committee for Standardization (CEN), Frontier Clinical Research
- EN ISO 14155-2:2009 Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans
- prEN 540-1992 Clinical investigation of medical devices for human subjects
國家藥監(jiān)局, Frontier Clinical Research
- YY/T 1754.1-2020 Preclinical Animal Studies for Medical Devices Part 1: General Requirements
GSO, Frontier Clinical Research
- OS GSO ISO 14155:2015 Clinical investigation of medical devices for human subjects -- Good clinical practice
- GSO ISO 29943-1:2021 Condoms — Guidance on clinical studies — Part 1: Male condoms, clinical function studies based on self-reports
- BH GSO ISO 29943-1:2022 Condoms — Guidance on clinical studies — Part 1: Male condoms, clinical function studies based on self-reports
- GSO ISO 29943-2:2021 Condoms — Guidance on clinical studies — Part 2: Female condoms, clinical function studies based on self-reports
KR-KS, Frontier Clinical Research
- KS P ISO 14155-2022 Clinical investigation of medical devices for human subjects — Good clinical practice
US-FCR, Frontier Clinical Research
British Standards Institution (BSI), Frontier Clinical Research
- BS ISO 29943-1:2017 Condoms. Guidance on clinical studies. Male condoms, clinical function studies based on self-reports
- BS ISO 29943-2:2017 Condoms. Guidance on clinical studies. Female condoms, clinical function studies based on self-reports
- BS EN 540:1993(1998) Clinicalinvestigationof medical devices for human subjects
- 24/30467406 DC BS EN ISO 14155 Clinical investigation of medical devices for human subjects - Good clinical practice
- BS EN ISO 11979-7:2006+A1:2012 Ophthalmic implants. Intraocular lenses. Clinical investigations
- BS EN ISO 11979-7:2014 Ophthalmic implants. Intraocular lenses. Clinical investigations
- 18/30344902 DC BS EN ISO 14155. Clinical investigation of medical devices for human subjects. Good clinical practice
ES-UNE, Frontier Clinical Research
- UNE-EN ISO 14155:2021 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)
US-HHS, Frontier Clinical Research
Association Francaise de Normalisation, Frontier Clinical Research
German Institute for Standardization, Frontier Clinical Research
- DIN EN ISO 14155:2021-05 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020); German version EN ISO 14155:2020
- DIN EN ISO 14155:2024 Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/DIS 14155:2024); German and English version prEN ISO 14155:2024
International Organization for Standardization (ISO), Frontier Clinical Research
- ISO 14155:2011 Clinical investigation of medical devices for human subjects - Good clinical practice
- ISO 29943-2:2017 Condoms - Guidance on clinical studies - Part 2: Female condoms, clinical function studies based on self-reports
- ISO 29943-1:2017 Condoms - Guidance on clinical studies - Part 1: Male condoms, clinical function studies based on self-reports
- ISO 14155:2011/cor 1:2011 Clinical investigation of medical devices for human subjects - Good clinical practice; Technical Corrigendum 1
NL-NEN, Frontier Clinical Research
- NEN-EN 540-1994 Clinical investigation of medical devices for human subjects
General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, Frontier Clinical Research
- GB/T 42168.1-2022 Condoms—Guidance on clinical studies—Part 1: Male condoms, clinical function studies based on self reports
GOST, Frontier Clinical Research
- GOST R ISO 14155-2022 Clinical investigation of medical devices for human subjects. Good clinical practice
Danish Standards Foundation, Frontier Clinical Research
- DS/EN 540:1993 Clinical investigation of medical devices for human subjects
- DS/EN ISO 14155:2013 Clinical investigation of medical devices for human subjects - Good clinical practice
PT-IPQ, Frontier Clinical Research
- NP EN 540-2001 Clinical investigation of medical devices for human subjects
Shanghai Provincial Standard of the People's Republic of China, Frontier Clinical Research
IT-UNI, Frontier Clinical Research
Beijing Provincial Standard of the People's Republic of China, Frontier Clinical Research
RU-GOST R, Frontier Clinical Research
US-AAMI, Frontier Clinical Research